Rare variants inTMEM132Din a case-control sample for panic disorder
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Rare variants inTMEM132Din a case-control sample for panic disorder
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
Volume 159B, Issue 8, Pages 896-907
Publisher
Wiley
Online
2012-08-22
DOI
10.1002/ajmg.b.32096
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Replication and meta-analysis of TMEM132D gene variants in panic disorder
- (2012) A Erhardt et al. Translational Psychiatry
- vipR: variant identification in pooled DNA using R
- (2011) A. Altmann et al. BIOINFORMATICS
- SHRiMP2: Sensitive yet Practical Short Read Mapping
- (2011) Matei David et al. BIOINFORMATICS
- Mapping Rare and Common Causal Alleles for Complex Human Diseases
- (2011) Soumya Raychaudhuri CELL
- dbNSFP: A lightweight database of human nonsynonymous SNPs and their functional predictions
- (2011) Xiaoming Liu et al. HUMAN MUTATION
- Genome-Wide Association Study of the Child Behavior Checklist Dysregulation Profile
- (2011) Eric Mick et al. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
- Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
- (2011) Gosia Trynka et al. NATURE GENETICS
- TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum
- (2011) Erica E Davis et al. NATURE GENETICS
- Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
- (2011) Manuel A Rivas et al. NATURE GENETICS
- The Neuronal Transporter Gene SLC6A15 Confers Risk to Major Depression
- (2011) Martin A. Kohli et al. NEURON
- Clustered Coding Variants in the Glutamate Receptor Complexes of Individuals with Schizophrenia and Bipolar Disorder
- (2011) René A. W. Frank et al. PLoS One
- Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population
- (2011) Lotte N. Moens et al. PLoS One
- Multiplexed resequencing analysis to identify rare variants in pooled DNA with barcode indexing using next-generation sequencer
- (2010) Jun Mitsui et al. JOURNAL OF HUMAN GENETICS
- TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies
- (2010) A Erhardt et al. MOLECULAR PSYCHIATRY
- Understanding mechanisms underlying human gene expression variation with RNA sequencing
- (2010) Joseph K. Pickrell et al. NATURE
- Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia
- (2010) Christopher T Johansen et al. NATURE GENETICS
- High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency
- (2010) Sarah E Calvo et al. NATURE GENETICS
- Statistical analysis strategies for association studies involving rare variants
- (2010) Vikas Bansal et al. NATURE REVIEWS GENETICS
- Uncovering the roles of rare variants in common disease through whole-genome sequencing
- (2010) Elizabeth T. Cirulli et al. NATURE REVIEWS GENETICS
- Missing heritability and strategies for finding the underlying causes of complex disease
- (2010) Evan E. Eichler et al. NATURE REVIEWS GENETICS
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- Reduced Expression of IFIH1 Is Protective for Type 1 Diabetes
- (2010) Kate Downes et al. PLoS One
- Genetic architecture of a complex trait and its implications for fitness and genome-wide association studies
- (2010) A. Eyre-Walker PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Rare Variants Create Synthetic Genome-Wide Associations
- (2010) Samuel P. Dickson et al. PLOS BIOLOGY
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- Common vs. rare allele hypotheses for complex diseases
- (2009) Nicholas J Schork et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Deep sequencing to reveal new variants in pooled DNA samples
- (2009) Astrid A. Out et al. HUMAN MUTATION
- Finding the missing heritability of complex diseases
- (2009) Teri A. Manolio et al. NATURE
- Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
- (2009) Prateek Kumar et al. Nature Protocols
- Human genetic variation and its contribution to complex traits
- (2009) Kelly A. Frazer et al. NATURE REVIEWS GENETICS
- Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes
- (2009) S. Nejentsev et al. SCIENCE
- Genome-wide association studies: potential next steps on a genetic journey
- (2008) M. I. McCarthy et al. HUMAN MOLECULAR GENETICS
- Personal genomes: The case of the missing heritability
- (2008) Brendan Maher NATURE
- Common and rare variants in multifactorial susceptibility to common diseases
- (2008) Walter Bodmer et al. NATURE GENETICS
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now